Drive 15021BV-LWRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383007694), received between Sep 12, 2024 and Sep 12, 2024 — classified as 1 death.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• DeathSep 12, 2024Break; Break

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A BED RAIL BY THE PROVIDER WHO STATED THAT THE END USER WAS HAVING NURSING CARE DONE WHEN THE BED RAIL COLLAPSED AND BROKE, AND THE END USER FELL TO THE FLOOR. THE END USER WAS ADMITTED TO THE HOSPITAL AND EXPIRED A WEEK OR TWO LATER, HOWEVER NO CAUSE OF DEATH WAS REPORTED. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

  Patient problems: Insufficient Information

  MAUDE report 20202502 ↗